Autor: |
Wang, Qi-Yuan, Sang, Li-Peng, Zhang, Zhen, Jiang, Yang, Tian, Hui, Zhao, Xia, Guo, Xiang, Li, Shi-Hui |
Předmět: |
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Zdroj: |
Chinese Journal of Polymer Science (Springer Science & Business Media B.V.); Feb2024, Vol. 42 Issue 2, p223-229, 7p |
Abstrakt: |
Coordination polymerization of renewable β-ocimene has been investigated using asymmetric diiminophosphinate lutetium complex 1, β-diketiminate yttrium complex 2, bis(phosphino)carbazolide yttrium complex 3, half-sandwich benzyl fluorenyl scandium complex 4 and pyridyl-methylene-fluorenyl rare-metal complexes 5a–5c. Complexes 1, 4 and 5a–5c show trans-1,2-regioselectivities and high activities, of which 5c exhibits excellent isoselectivity (mmmm>99%). Conversely, complexes 2 and 3 promote β-ocimene polymerization to produce isotactic cis-1,4-polyocimenes (cis-1,4>99%, mm>95%). Diblock copolymers cis-1,4-PIP-block-cis-1,4-POc and cis-1,4-PBD-block-cis-1,4-POc are obtained in one-pot reactions of β-ocimene with isoprene and butadiene using complex 3. Epoxidation and hydroxylation of polyocimene afford functionalized polyolefins with enhanced Tg (from −20 °C to 79 °C and 74 °C) and hydrophilicity. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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